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Associations of MMP-2 −1306 C/T and MMP-9 −1562 C/T polymorphisms with breast cancer risk among different populations: a meta-analysis

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Abstract

The meta-analysis aims to investigate association between two matrix metalloproteinases (MMPs) polymorphisms (MMP-2 −1306 C/T and MMP-9 −1562 C/T) and breast cancer risk. Eligible studies were retrieved from relevant databases, based on predefined criteria. Quality assessment was evaluated by Newcastle–Ottawa Scale. Odds ratio (OR) with its 95% confidence interval (CI) was selected as the effect size for the meta-analysis. As a result, 13 studies were included. MMP-2 −1306 C/T polymorphism was not significantly associated with breast cancer risk under all genetic models (P > 0.05). However, subgroup analysis stratified by ethnicity showed a significant association between MMP-2 −1306 C/T polymorphism and reduced breast cancer risk in Asian populations under allelic model (OR 0.60, 95% CI 0.39–0.90, P = 0.02) and dominant model (OR 0.55, 95% CI 0.34–0.89, P = 0.02). MMP-9 −1562 C/T polymorphism was significantly related to increased breast cancer risk under allelic model (OR 1.50, 95% CI 1.06–2.12, P = 0.02), additive model (OR 1.45, 95% CI 1.02–2.05, P = 0.04) and recessive model (OR 1.54, 95% CI 1.13–2.12, OR 0.007). A significant association between MMP-9 −1562 C/T polymorphism and increased breast cancer risk in Caucasian was detected under most of the genetic models (P < 0.05). MMP-2 −1306 C/T polymorphism might be significantly associated with reduced breast cancer risk in Asian, while MMP-9 −1562 C/T might be closely related to increased breast cancer risk, especially in Caucasian.

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Correspondence to Meng Han.

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Meng Han, Qingfeng Yang, Kai Feng, Rongping Li, Jia Ren, and Liguang Wei declares that they have no conflict of interest.

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In this study, no tissue or sample was obtained from human or animal. This study was compliant with ethical standards.

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Han, M., Yang, Q., Feng, K. et al. Associations of MMP-2 −1306 C/T and MMP-9 −1562 C/T polymorphisms with breast cancer risk among different populations: a meta-analysis. Genes Genom 39, 331–340 (2017). https://doi.org/10.1007/s13258-016-0498-z

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  • DOI: https://doi.org/10.1007/s13258-016-0498-z

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